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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482258Generated: October 26, 2026

Sodium hydride → 3-Methyl-7-(methylpivaloyl)xanthine

https://huagongshe.com/reaction/482258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-MethylxanthineHCID 70639—
Reactant1-(5-Ketohexyl)-3-methylxanthineHCID 15023898—
Reactant4-Chloro-2,2-dimethylbutanoateHCID 21753047—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-Methyl-7-(methylpivaloyl)xanthineHCID 2158423390%

Reaction Steps

This example illustrates a method for synthesis of CT1505 (1-(5-oxohexyl)-3-methylxanthine). A mixture of 3-methylxanthine (1.00 g, 6.0 mmol) and NaH (145 mg, 6.0 mmol) in DMSO (dimethyl sulfoxide) (20 ml) was stirred until homogeneous (about 30 min). Chloromethylpivalate (865 μl, 904 mg, 6.0 mmol) was added and the reaction mixture was stirred for 18 hrs. The reaction mixture was poured into 70 ml of water and extracted with 25% ethanol/dichloromethane (4×60 ml). The combined organic extracts were combined, dried with sodium sulfate, and then evaporated in a rotoevaporator to a volume of 40 ml. The solution was cooled in ice water and it formed a thick, white precipitate. The solid was filtered off under suction and dried under vacuum to give the 3-methyl-7-(methylpivaloyl)xanthine (1.43 g, 5.4 mmol, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05795897
Source datasetuspto-grants-1998_08
ORD IDord-c0b5bd0b04e8470b9dc18c6a16097b15
Source noteuspto-grants-1998_08